Term:hypotrichosis 7
go back to main search page
Accession:DOID:0110704 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal recessive mutation of LIPH on chromosome 3q27.2. (DO)
Synonyms:exact_synonym: HYPT7;   Hypotrichosis, Autosomal Recessive;   Hypotrichosis, Localized, Autosomal Recessive, 2;   LAH2;   Mari type Alopecia universalis congenita;   Total Hypotrichosis, Mari Type
 primary_id: MESH:C536973
 alt_id: DOID:9000861;   OMIM:604379;   RDO:0002708;   RDO:9003979
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants       view all columns           Sort by:
hypotrichosis 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Liph lipase H JBrowse link 11 82,680,167 82,732,145 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          hypotrichosis 7 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      nervous system disease 9154
        sensory system disease 4267
          skin disease 2270
            hair disease 214
              hypotrichosis 98
                alopecia 77
                  hypotrichosis 7 1
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.